TOPO™ TA Cloning™ Kit for Sequencing, with One Shot™ TOP10 Chemically Competent E. coli (Supply Center Packaging)
TOPO&trade; TA Cloning&trade; Kit for Sequencing, with One Shot&trade; TOP10 Chemically Competent <i>E. coli</i> (Supply Center Packaging)
Invitrogen™

TOPO™ TA Cloning™ Kit for Sequencing, with One Shot™ TOP10 Chemically Competent E. coli (Supply Center Packaging)

The TOPO™ TA Cloning™ Kits for Sequencing provide a highly efficient, 5-minute, one-step cloning strategy ('TOPO™ Cloning') for the directRead more
Have Questions?
Catalog NumberQuantity
K457501SC25 Reactions
Catalog number K457501SC
Price (CLP)
933.965
Each
Add to cart
Quantity:
25 Reactions
Price (CLP)
933.965
Each
Add to cart
The TOPO™ TA Cloning™ Kits for Sequencing provide a highly efficient, 5-minute, one-step cloning strategy ('TOPO™ Cloning') for the direct insertion of Taq polymerase–amplified PCR products into a plasmid vector for sequencing. Each kit uses the pCR™4-TOPO™ TA vector with specially designed sequencing primer sites that return more insert sequence and less vector sequence from each reaction, and are available with a variety of competent cells, or no competent cells, depending on your needs and budget. These kits include everything necessary to clone and select recombinant vectors containing your PCR fragment of choice. This product comes in Supply Center packaging, which features an additional outer box that holds both the TOPO™ vector box and the competent cells box. This special packaging helps ensure that visitors to a Supply Center obtain the complete kit.

Features of TOPO™ TA Cloning™ Kits for Sequencing:

Get more sequence—allows for more insert sequence and less vector seuquence when using standard sequencing primers
Fast and easy—go from PCR to clones in just 3 steps and in as little as 5 minutes hands-on time
Efficient—obtain up to 95% clones with correct insert
Proven—reliable performance for over a decade with over 4,000 citations

TOPO™ TA Cloning™ Kits for Sequencing—overview

Vector: pCR™4-TOPO™ TA vector—optimized cloning vector for improved sequencing results

Cloning method: TOPO™ TA Cloning™—Topoisomerase I–based, 5-minute ligation of PCR products with 3´A overhangs (Taq-amplified) to the vector

Competent cells: Various options—choose from kits with general, high-efficiency, bacteriophage T1-resistant, or fast-growing competent cells, or use your own

pCR™4-TOPO™ TA vectoroptimized for sequencing
We have removed much of the multiple cloning site from the pCR™4-TOPO™ TA vector to shorten the distance between sequencing primer sites and the insert site to as little as 33 bp. This means sequencing reactions give less vector sequence and more insert sequence. The pCR™4-TOPO™ TA vector has sites for 4 common sequencing primers: M13 forward, M13 reverse, T7, and T3. The kits include an aliquot of each.

pCR™4-TOPO™ TA clone selection and manipulation
The pCR™4-TOPO™ TA vector contains both ampicillin and kanamycin resistance markers and a LacZα-ccdB gene fusion for positive selection and blue/white screening. The vector’s minimized multiple cloning site still includes flanking EcoRI sites for simplified excision of cloned PCR products and a unique Sse8387I site for generation of nested deletions prior to sequencing. T7 and T3 promoters are also present for in vitro transcription.

Simplified TOPO™-based cloning
Using TOPO™ cloning technology, there is no need for PCR primers containing specific sequences, post-PCR procedures, vector preparation, or other time-intensive DNA manipulation steps. Just add your PCR reaction straight to the provided topoisomerase-charged vector, incubate 5 minutes, and transform with the providedE. coli competent cells.

Efficient cloning
With up to 95% of clones carrying the desired insert, you can screen less clones and save time and money. The pCR™4-TOPO™ TA vector used in this kit comes with 3´T overhangs for efficient ligation of Taq-amplified PCR products, which contain 3´A overhangs.

The standard in cloning
When it comes to cloning, TOPO™ cloning technology has been a reliable partner for thousands of scientists for over ten years. Fast, simple-to-use, and efficient, TOPO™ cloning has been applied to many different vectors for a wide array of applications.

TOPO™ TA Cloning™ Kits for Sequencing—kit options
The TOPO™ TA Cloning™ Kit for Sequencing can be purchased with a variety of competent cells that deliver different advantages depending upon your needs:

• General cloning: TOP10 (Cat. No. K4575-J10, K4575-01, K4575-40)
• High-efficiency cloning: TOP10 Electrocomp™ Cells (Cat. No. K4580-01, K4580-40)
• General cloning, bacteriophage T1 resistance: DH5α-T1R (Cat. No. K4595-01, K4595-40)
• Fast growth: Mach1™-T1R Chemically Competent E. Coli (Cat. No. K4530-20)
• Provide your own: for flexibility and to save money (Cat. No. 450030)

We also offer a version of the kit that includes a PureLink™ Quick Plasmid Miniprep Kit (Cat. No. K4575-02) for use in isolation of clean, sequencing-ready, recombinant plasmid.

Related Links

Custom Vector Construction and Cloning Services
Plasmid DNA Purification Kit Selection Guide
PCR Reagents, Instruments, and Supplies
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Bacterial or Yeast StrainTOP10
Cell TypeChemically Competent
Cloning MethodTOPO™-TA
Product LineOne Shot
Product TypeCloning Kit
PromoterT7, T3
Quantity25 Reactions
Shipping ConditionDry Ice
VectorTOPO-TA Cloning Vectors
FormatKit
Unit SizeEach
Contents & Storage
Box 1:
• Topoisomerase I-activated pCR™4-TOPO™ vector
• PCR buffer
• Salt solution
• dNTPs
• Control template
• T3, T7, M13 forward, and M13 reverse primers
• Control PCR primers
• Sterile water

Store at -5 to -30°C.
All reagents are stable for 6 months when properly stored.

Box 2:
• One Shot™ Chemically Competent or Electrocomp™ E. coli
• S.O.C. medium
• Supercoiled pUC19 control plasmid

Store at -68 to -85°C.

Frequently asked questions (FAQs)

Can I store my competent E. coli in liquid nitrogen?

We do not recommend storing competent E. coli strains in liquid nitrogen as the extreme temperature can be harmful to the cells. Also, the plastic storage vials are not intended to withstand the extreme temperature and may crack or break.

How should I store my competent E. coli?

We recommend storing our competent E. coli strains at -80°C. Storage at warmer temperatures, even for a brief period of time, will significantly decrease transformation efficiency.

What is the difference between the pCR2.1-TOPO and pCR4-TOPO vectors?

The vector backbones for both of these vectors are very similar. The main difference is that the pCR4-TOPO vector has sequencing primer sites located as close as 33 base pairs from the PCR product insertion site. This minimizes the amount of vector DNA sequence that needs to be read before reaching the sequence of the insert, making the pCR4-TOPO vector very useful for sequencing applications.

What is the difference between the pCR2.1-TOPO and pCRII-TOPO vectors?

The vector backbones for both of these vectors are very similar. The main difference is that the pCRII-TOPO vector is a dual promoter vector, containing the SP6 and T7 promoters for in vitro transcription/sequencing, whereas the pCR2.1-TOPO vector contains only the T7 promoter for in vitro transcription/sequencing. Both vectors contain the M13 Forward and Reverse primer sites for sequencing or PCR screening.

Your TOPO cloning kits contain a control template and control primers. Can I obtain the sequence of the control template?

The sequence of the control template is proprietary.

Citations & References (6)

Citations & References
Abstract
Molecular cloning and characterization of Foxp3 in Atlantic salmon (Salmo salar).
Authors:Zhang Z, Chi H, Niu C, Bøgwald J, Dalmo RA,
Journal:Fish Shellfish Immunol
PubMed ID:21276855
'Foxp3 is a T cell-specific transcription factor and plays a key role in the development of Treg cells and in the immune regulatory process during inflammation. Here we report cloning and characterization of the full-length cDNA of Atlantic salmon Foxp3, which possesses a Forkhead domain, a zinc finger domain and ... More
Detection of cytosine methylation in RNA using bisulfite sequencing.
Authors:Pollex T, Hanna K, Schaefer M
Journal:Cold Spring Harb Protoc
PubMed ID:20889702
'Post-transcriptional RNA modifications are a characteristic feature of noncoding RNAs and have been described for ribosomal RNAs (rRNAs), transfer RNAs (tRNAs), and various other small RNAs. However, the biological function of most of these modifications remains uncharacterized. Cytosine-5 methylation (5mC) has been detected in abundant and long-lived RNA molecules such ... More
Unique DNA methylome profiles in CpG island methylator phenotype colon cancers.
Authors:Xu Y, Hu B, Choi AJ, Gopalan B, Lee BH, Kalady MF, Church JM, Ting AH
Journal:Genome Res
PubMed ID:21990380
'A subset of colorectal cancers was postulated to have the CpG island methylator phenotype (CIMP), a higher propensity for CpG island DNA methylation. The validity of CIMP, its molecular basis, and its prognostic value remain highly controversial. Using MBD-isolated genome sequencing, we mapped and compared genome-wide DNA methylation profiles of ... More
Enhanced autointegration in hyperstable simian immunodeficiency virus capsid mutants blocked after reverse transcription.
Authors:Tipper C, Sodroski J
Journal:J Virol
PubMed ID:23345510
'After entering a host cell, retroviruses such as simian immunodeficiency virus (SIV) uncoat, disassembling the viral capsid. Rates of uncoating that are too high and too low can be detrimental to the efficiency of infection. Rapid uncoating typically leads to blocks in reverse transcription, but the basis for replication defects ... More
Thioredoxin 1 is responsible for antibody disulfide reduction in CHO cell culture.
Authors:Koterba KL, Borgschulte T, Laird MW
Journal:J Biotechnol
PubMed ID:22138638
During large-scale manufacturing of an IgG1 monoclonal antibody in Chinese hamster ovary (CHO) cells, reduction of the antibody's disulfide bonds was observed. We present evidence that mammalian thioredoxin 1 (TXN1) is the terminal enzyme responsible for this reduction event. We demonstrate a marked prevention of IgG1 disulfide bond reduction in ... More